510(k) K123752 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ACCULIF TL AND PL CAGE
| Applicant | Coalign Innovations, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jan 14, 2013 |
| Received | Dec 6, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123752
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.